Clinical Research project Manager #HCK
Summary
Oversee clinical research studies from planning to closeout, coordinating with sponsors, ethics boards, and monitors while managing timelines, budgets, and compliance with GCP standards.
Responsibilities
• To oversee full study lifecycle from planning to closeout.
• To act as primary liaison between the clinical research sponsors ethics boards, and monitors.
• To lead protocol development to ensure operational feasibility.
• To manage study documents, risk mitigation, safety oversight, and trial master files.
• To coordinate study timelines, vendor engagement, training and logistics
• To Track budgets and provide regular study updates to stakeholders.
• To Coordinate monitoring visits and resolve data queries and quality issues.
Qualification
Degree in Nursing, Science, Health, or Management.
• Minimum 5 years of clinical research experience.
• Strong knowledge of GCP and clinical trial processes.
Interested candidates please send in your resume to: recruitment@recruitexpress.com.sg
EA Personnel: Valerie Yong Kian Fung
CEI No.: R1103704
Recruit Express Pte Ltd, EA License No.: 99C4599